Hannah Klinkhammer

Philipps University of Marburg — Germany

Biochemistry, Genetics and Molecular Biology · Life Sciences

11h-index606citations57works3.02yr avg
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Research Topics

Genomics and Rare Diseases(18), Genetic Associations and Epidemiology(14), Genomic variations and chromosomal abnormalities(11), Genetic and phenotypic traits in livestock(9), Genetic factors in colorectal cancer(9)

Publications57 total

Polygenic Risk Scores of COPD Predict Lung Function Decline and Early COPD: Results from COSYCONET
American Journal of Respiratory and Critical Care Medicine·2026Open Access
Associations Between Structural Phenotype and Polygenic Risk Scores in Intermediate Age-Related Macular Degeneration – A MACUSTAR Report
Translational Vision Science & Technology·2025Open Access
Detecting gene-environment interactions to guide personalized intervention: boosting distributional regression for polygenic scores
arXiv (Cornell University)·2025Open Access
Author Correction: Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Nature Genetics·2025Open Access
Evidence for a transgenerational mutational signature from ionizing radiation exposure in humans
Scientific Reports·2025Open Access
Enhanced Variable Selection for Boosting Sparser and Less Complex Models in Distributional Copula Regression
Statistics in Biosciences·2025· 1 citedOpen Access
Artificial intelligence-driven genotype–epigenotype–phenotype approaches to resolve challenges in syndrome diagnostics
EBioMedicine·2025· 2 citedOpen Access
Coupling deep phenotypic quantification with next-generation phenotyping for 192 individuals with germline histonopathies
Human Genetics and Genomics Advances·2025· 2 citedOpen Access
Boosting distributional copula regression for bivariate binary, discrete and mixed responses
Statistical Methods in Medical Research·2025· 2 citedOpen Access
Effectiveness of Technology-Supported Ultrasound Training in Prenatal Diagnosis through an Adaptive Image Recognition Training System (AdaptUS)
Geburtshilfe und Frauenheilkunde·2025· 2 citedOpen Access
Leveraging next-generation phenotyping for ACMG classification from VUS to likely pathogenic in Mowat-Wilson syndrome
2025Open Access
Homozygous variant in translocase of outer mitochondrial membrane 7 leads to metabolic reprogramming and microcephalic osteodysplastic dwarfism with moyamoya disease
EBioMedicine·2024· 5 citedOpen Access
Genetic Prediction Modeling in Large Cohort Studies via Boosting Targeted Loss Functions
Statistics in Medicine·2024Open Access
F55. LOSS-OF-FUNCTION VARIANTS IN CUL3 CAUSE A SYNDROMIC NEURODEVELOPMENTAL DISORDER
European Neuropsychopharmacology·2024
Loss‐of‐Function Variants in <scp><i>CUL3</i></scp> Cause a Syndromic Neurodevelopmental Disorder
Annals of Neurology·2024· 9 citedOpen Access
Transferability of polygenic risk scores depending on demography and dominance coefficients
2024· 1 citedOpen Access
Next-generation phenotyping integrated in a national framework for patients with ultrarare disorders improves genetic diagnostics and yields new molecular findings
Nature Genetics·2024· 34 citedOpen Access
GestaltMatcher Database - A global reference for facial phenotypic variability in rare human diseases
2024· 3 citedOpen Access
Enhanced variable selection for boosting sparser and less complex models in distributional copula regression
arXiv (Cornell University)·2024Open Access
Generalizability of polygenic prediction models: how is the R2 defined on test data?
BMC Medical Genomics·2024· 7 citedOpen Access
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Frequent Co-authors

Peter Krawitz(31), Andreas Mayr(21), Tzung‐Chien Hsieh(17), Carlo Maj(16), Alexej Knaus(11), Shahida Moosa(10), Hellen Lesmann(10), Christian Staerk(10), Claudia Perne(9), Theresa Brunet(9), Sugirthan Sivalingam(8), Axel Schmidt(8), Luisa Averdunk(8), Emadeldin Hassanin(8), Magdalena Danyel(7), Isabel Spier(7), Jean Tori Pantel(6), Alexander Hustinx(6), Rana Aldisi(6), Martin A. Mensah(5)